chloroformamidine hydrochloride

COC(=O)C(=Cc1ccc(C#N)cc1OC[C@@H](CCC(=O)OCc1ccccc1)NC(=O)c1cccc(-c2ccc(NC(=N)N)cc2)c1)NC(C)=O.O=C(O)C(F)(F)F
Reaction #78214
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Nc1nc(N)c2c(Cl)c(-c3cc(Cl)cc(Cl)c3)ccc2n1
Reaction #80905
2,4-diamino-5-chloro-6-(3,5-dichlorophenyl)quinazoline
收率 29.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1c(C(Cl)=Cc2ccc(C(F)(F)F)cc2)ccc2nc(N)nc(N)c12
Reaction #80919
2,4-diamino-5-methyl-6-[1-chloro-2-(4-trifluoromethylphenyl)ethenyl]quinazoline
收率 46.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cccc2nc(N)nc(N)c12
Reaction #80935
2,4-diamino-5-methylquinazoline
收率 86.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1nc(=O)c2sc3c(c2[nH]1)CCCC3
Reaction #302927
desired compound
收率 95.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Nc1nc(N)c2c(-c3ccc([N+](=O)[O-])cc3)csc2n1
Reaction #314813
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Nc1nc(N)c2c(Cl)c(-c3cc(Cl)cc(Cl)c3)ccc2n1
Reaction #450943
2,4-diamino-5-chloro-6-(3,5-dichlorophenyl)quinazoline
收率 29.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
Cc1c(C(Cl)=Cc2ccc(C(F)(F)F)cc2)ccc2nc(N)nc(N)c12
Reaction #450957
2,4-diamino-5-methyl-6-[1-chloro-2-(4-trifluoromethylphenyl)ethenyl]quinazoline
收率 46.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
Cc1cccc2nc(N)nc(N)c12
Reaction #450972
2,4-diamino-5-methylquinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
Cc1nc2nc(N)nc(N)c2nc1C(=O)c1ccccc1
Reaction #528081
2,4-diamino-7-methyl-6-phenylcarbonylpteridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
Nc1nc(N)c2nc(C(Cl)=Cc3ccc(C(F)(F)F)cc3)cnc2n1
Reaction #528085
2,4-diamino-6-[1-chloro-2-(4-trifluoromethylphenyl)ethenyl]pteridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
Nc1nc2[nH]c3cccc(Cl)c3c2c(=O)[nH]1
Reaction #627042
2-Amino-5chloro-3,9-dihydro-4H-pyrimido[4,5-b]indol-4-one
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
Nc1nc(=O)c2c(-c3ccc(F)cc3)csc2[nH]1
Reaction #675925
title compound
收率 111.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1sc2[nH]c(N)nc(=O)c2c1-c1ccccc1
Reaction #675926
title compound
收率 94.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1csc2[nH]c(N)nc(=O)c12
Reaction #675928
title compound
收率 87.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCCCCCC=Cc1ccc2nc(N)nc(N)c2c1C
Reaction #707188
white solid
收率 78.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
Cc1c(C#N)ccc2nc(N)nc(N)c12
Reaction #740718
2,4-diamino-5-methyl-6-quinazolinecarbonitrile
收率 43.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_06
Nc1nc2sccc2c(=O)[nH]1
Reaction #805489
title compound
收率 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Nc1nc2sc(-c3ccc(F)cc3)cc2c(=O)[nH]1
Reaction #805496
title compound
收率 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Nc1nc2sccc2c(=O)[nH]1
Reaction #805499
crude title compound
收率 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
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